# K241199: Rotatable Connector (5944RL)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Launch Electrical Co., Ltd.
- Decided: Jan 23, 2025 after 268 days
- Product code: LDF (Electrode, Pacemaker, Temporary)
- Device class: 2
- Regulation: 21 CFR 870.3680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K923407 (1992). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K923407: Medtronic Models 5455L and 5455SL Surgical Cables, Medtronic Vascular (1992) Summary page 6.

## Indications for use
The rotatable connector is intended for use as part of a temporary cardiac pacing system. It connects a cardiovascular stimulating instrument to a cardiac pacing lead. It is intended for use by trained clinicians in a clinical environment.

Source page: https://510kreport.com/device/K241199
Methodology: https://510kreport.com/methodology